Canonical Allele Identifier: PA2825003031
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2264696
ClinVar RCV Id: RCV004116513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000005.3:p.Ile1005Thr
CA6438236
NM_000014.6:c.3014T>C